Polyolefin waste to light olefins with ethylene and base-metal heterogeneous catalysts

Author:

Conk Richard J.12ORCID,Stahler Jules F.1ORCID,Shi Jake X13ORCID,Yang Ji3ORCID,Lefton Natalie G.2,Brunn John N.1ORCID,Bell Alexis T.32ORCID,Hartwig John F.13ORCID

Affiliation:

1. Department of Chemistry, University of California, Berkeley, Berkeley, CA 94720, USA.

2. Department of Chemical and Biomolecular Engineering, University of California, Berkeley, Berkeley, CA 94720, USA.

3. Division of Chemical Sciences, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

Abstract

The selective conversion of polyethylene, polypropylene, and mixtures of the two polymers to form products with high volume demand is urgently needed because current methods suffer from low selectivity, produce large quantities of greenhouse gases, or rely on expensive, single-use catalysts. The isomerizing ethenolysis of unsaturated polyolefins could be an energetically and environmentally viable route to propylene and isobutylene, but noble-metal homogeneous catalysts and an unsaturated polyolefin are currently required, and the process has been limited to polyethylene. We show that the simple combination of tungsten oxide on silica and sodium on gamma-alumina transforms polyethylene, polypropylene, or a mixture of the two, including post-consumer forms of these materials, to propylene or a mixture of propylene and isobutylene in greater than 90% yield at 320°C without the need for dehydrogenation of the starting polyolefins.

Publisher

American Association for the Advancement of Science (AAAS)

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